Ionic liquids (ILs) have attracted considerable attention in several sectors (from energy storage to catalysis, from drug delivery to separation media) owing to their attractive properties, such as ...high thermal stability, wide electrochemical window, and high ionic conductivity. However, their high viscosity and surface tension compared to conventional organic solvents can lead to unfavorable transport properties. To circumvent undesired kinetics effects limiting mass transfer, the discretization of ILs into small droplets has been proposed as a method to increase the effective surface area and the rates of mass transfer. In the present review paper, we summarize the different methods developed so far for encapsulating ILs in organic or inorganic shells and highlight characteristic features of each approach, while outlining potential applications. The remarkable tunability of ILs, which derives from the high number of anions and cations currently available as well as their permutations, combines with the possibility of tailoring the composition, size, dispersity, and properties (
e.g.
, mechanical, transport) of the shell to provide a toolbox for rationally designing encapsulated ILs for next-generation applications, including carbon capture, energy storage devices, waste handling, and microreactors. We conclude this review with an outlook on potential applications that could benefit from the possibility of encapsulating ILs in organic and inorganic shells.
Encapsulated ionic liquids (ILs) are candidate materials for several applications owing to the attractive properties of ILs combined with the enhanced mass transfer rate obtained through the discretization of ILs in small capsules.
Control over faceting in nanocrystals (NCs) is pivotal for many applications, but most notably when investigating catalytic reactions which occur on the surfaces of nanostructures. Anatase titanium ...dioxide (TiO(2)) is one of the most studied photocatalysts, but the shape dependence of its activity has not yet been satisfactorily investigated and many questions still remain unanswered. We report the nonaqueous surfactant-assisted synthesis of highly uniform anatase TiO(2) NCs with tailorable morphology in the 10-100 nm size regime, prepared through a seeded growth technique. Introduction of titanium(IV) fluoride (TiF(4)) preferentially exposes the {001} facet of anatase through in situ release of hydrofluoric acid (HF), allowing for the formation of uniform anatase NCs based on the truncated tetragonal bipyramidal geometry. A method is described to engineer the percentage of {001} and {101} facets through the choice of cosurfactant and titanium precursor. X-ray diffraction studies are performed in conjunction with simulation to determine an average NC dimension which correlates with results obtained using electron microscopy. In addition to altering the particle shape, the introduction of TiF(4) into the synthesis results in TiO(2) NCs that are blue in color and display a broad visible/NIR absorbance which peaks in the infrared (λ(max) ≈ 3400 nm). The blue color results from oxygen vacancies formed in the presence of fluorine, as indicated by electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) studies. The surfactants on the surface of the NCs are removed through a simple ligand exchange procedure, allowing the shape dependence of photocatalytic hydrogen evolution to be studied using monodisperse TiO(2) NCs. Preliminary experiments on the photoreforming of methanol, employed as a model sacrificial agent, on platinized samples resulted in high volumes of evolved hydrogen (up to 2.1 mmol h(-1) g(-1)) under simulated solar illumination. Remarkably, the data suggest that, under our experimental conditions, the {101} facets of anatase are more active than the {001}.
The surface chemistry of amorphous zinc polyphosphates of different compositions (ranging from zinc metaphosphate to zinc orthophosphate) has been investigated by means of X-ray photoelectron ...spectroscopy (XPS) and time-of-flight secondary-ion mass spectroscopy (ToF-SIMS). The identification of the chain length of zinc polyphosphates by XPS was on the basis of the integrated intensity ratio of the bridging (P–O–P) and nonbridging (P = O and P–O–M) oxygen peaks used for fitting the oxygen 1s signal, the shift of the P 2p
3/2
signal towards lower binding energies and the modified Auger parameter towards higher values as the zinc content increases. The discrimination of the polyphosphate chain lengths was also achieved by ToF-SIMS, by comparing the intensities of selected characteristic phosphate fragments. Both techniques appear to be suitable for the investigation of polyphosphate glasses in applications such as tribology, where there is a need to identify the chain length present in the outermost monolayer of the film. Fourier-transform infrared (FT-IR) spectroscopy was used to characterize the bulk compounds. The FT-IR studies showed that long-chain structures linked through P–O–P bonds predominate in the metaphosphate composition, while when the zinc content is increased, the chains become shorter, ultimately being replaced by PO
4
monomers in the orthophosphate composition.
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•Imidazolium-based ionic liquids (ILs) were encapsulated in methacrylate polymer microcapsules.•Polymer-encapsulated ILs were dispersed in non-polar oils at concentration that exceeds ...their solubility limit.•Polymer-encapsulated ILs led to a reduction of friction in steel/steel sliding contacts.•Encapsulated imidazolium-based IL does not tribochemically react at steel surfaces.
While ionic liquids (ILs) have attracted much attention as potential next-generation lubricant additives, their implementation in oil formulations has been hindered by their limited solubility in hydrocarbon fluids and corrosivity. Here, we encapsulate an oil-insoluble IL that has been studied in lubrication science, namely 1-hexyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (HMIMTFSI), within poly(ethylene glycol dimethacrylate-buytl methacrylate copolymer) (poly(EGDM-c-BMA)) microshells using a mini-emulsion polymerization process. The synthesized poly(EGDM-c-BMA)-encapsulated HMIMTFSI microparticles are shown to be dispersible in a non-polar, synthetic oil (i.e., poly-α-olefin). Tribological experiments indicated that the microcapsules act as an additive reservoir that reduces friction by releasing the encapsulated IL at the sliding interface following the mechanical rupture of the polymer shell. X-ray photoelectron spectroscopy (XPS) measurements provided evidence that HMIMTFSI does not tribochemically react on steel surfaces to create a reaction layer, thus suggesting that this IL reduces friction by generating a solid-like, layered structure upon nanoconfinement at sliding asperities, as proposed by previous nanoscale studies. The results of this work do not only provide new insights into the lubrication mechanism of ILs when used as additives in base oils in general, but also establish a new, broadly-applicable framework based on polymer encapsulation for utilizing ILs or other compounds with limited solubility as additives for oil formulations.
Zinc polyphosphate glasses are the principal component of the antiwear tribofilms formed on steel surfaces in the presence of additives, such as zinc dialkyldithiophosphates. In this work, amorphous, ...zinc metaphosphate glasses have been synthesized and characterized by means of X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), elemental analysis, and X-ray photoelectron spectroscopy (XPS). Tribological tests were performed by rubbing steel balls against the zinc metaphosphate discs in a poly-α-olefin (PAO) bath at room temperature. XPS was used in order to characterize the tribostressed areas on both metaphosphate discs and steel balls. A transfer film, constituted of iron and zinc polyphosphates, was formed on the contact area of the balls. This transfer film was found to reduce friction and prevent ball wear. A reduction in the relative intensities of XPS signals related to bridging-oxygen species and a binding energy shift of 0.4 eV of the P 2p toward lower values demonstrated the presence of shorter-chain-length phosphates inside the tribo-tracks on the discs. Furthermore, iron was transferred to the glass during the tribological tests. A tribochemical reaction between zinc metaphosphate and iron oxide has been proposed as an explanation for the depolymerization of the glass and the formation of iron phosphate.
To investigate the chemical changes occurring at metal/lubricant interfaces under tribological conditions in the boundary-lubrication regime, an in situ system for conducting quantitative ...tribological measurements has been constructed by combining an attenuated total reflection Fourier-transform infrared (ATR/FT-IR) spectrometer with a reciprocating tribometer. By periodically acquiring ATR/FT-IR spectra during sliding, spectroscopic changes due to thermal and/or tribochemical reactions occurring at the metal/oil interface can be monitored and correlated with friction measurements. The usefulness of this tribological test system has been demonstrated by performing ATR tribological experiments in the presence of a poly-α-olefin base oil at high temperature (423 K) on iron-coated germanium ATR crystals.
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